Prune power: study tests if dried plums boost bone health in older women
NCT ID NCT07222111
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how eating dried plums (prunes) might help reduce bone loss in women after menopause. Researchers want to know if prunes change immune cell function and gut bacteria. Thirty women aged 60-75 will eat prunes or their normal diet for four weeks at a time, and provide blood and stool samples. The goal is to understand the connection between diet, gut health, and bone strength.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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60 to 75 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * women 60-75 years of age at the start of the study; * 12 or more consecutive months without a menstrual period; * willing to include dried plums in their daily diet and collect fecal samples at four time points; * ambulatory without assistance; * capacity to give informed consent. Exclusion Criteria: * women who have been on medications known to alter bone or calcium metabolism (e.g., oral bisphosphonates, raloxifene, denosumab, intermittent parathyroid hormone, growth hormone) within 12 months of starting the study. Prior use of intravenous bisphosphonates at any time. * women who have been on hormone replacement therapy, steroids (i.e., glucocorticoids), biologics, or chronic NSAID within 3 months of starting the study. * women with a previous diagnosis of osteoporosis (i.e., BMD T-score or history of vertebral fracture or fragility fractures of hip, wrist, humerus after the age of 50 yr) or other metabolic bone disease (e.g., osteomalacia or osteogenesis imperfect), renal disease, stroke, heart attack, type 2 diabetes, liver disease or autoimmune diseases (e.g., rheumatoid arthritis, systemic Lupus erythematosus, type 1 diabetes mellitus, IBD) that could affect bone metabolism or T cell biology will be excluded. * women who have undergone treatment for cancer within 12 months of starting the study * women who have been taking prebiotic or probiotic supplements or natural products that have estrogen-like effects in the past 3 months * women who smoke, have a BMI \>40 kg/m2 or \<18.5 kg/m2, or consume \>2 alcoholic drinks per day * women who regularly consume dried plums or prune juice (\>1 serving weekly).
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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Contacts and locations
Locations
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IU Health University Hospital Clinical Research Center
RECRUITINGIndianapolis, Indiana, 46202, United States